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Dr. Humberto Reyes B.

METABOLISMO DE LA BILIRRUBINA, PATOGENIA DE LAS ICTERICIAS. Dr. Humberto Reyes B. Síndrome de Criggler-Najjar : Déficit congénito de glucuronil transferasa Total (niño a la izquierda, con Kernicterus) Parcial (niño a la derecha). Laboratorio bioquímico hepático.

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Dr. Humberto Reyes B.

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  1. METABOLISMO DE LA BILIRRUBINA, PATOGENIA DE LAS ICTERICIAS Dr. Humberto Reyes B.

  2. Síndrome de Criggler-Najjar: • Déficit congénito de glucuronil transferasa • Total (niño a la izquierda, con Kernicterus) • Parcial (niño a la derecha)

  3. Laboratorio bioquímico hepático • Bilirrubinemia total y directa • Bilirrubina en orina • Aminotransferasas: Transaminasa pirúvica (SGPT) (ALAT) Transaminasa oxaloacética (SGOT) (ASAT) • Fosfatasas alcalinas • Gammaglutamil transpeptidasa (GGT) • Tiempo de protrombina • Albúmina sérica Esquema hepatítico Esquema colestásico

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